Associate Director, Quality Assurance - CDMO
The Associate Director of Quality Assurance is responsible for leading the Veranova Quality Assurance team, managing quality oversight of the manufacturing process and operations. This includes leading and managing multiple QA teams for batch record review, batch disposition, and on the floor QA support to ensure GMP compliance across all stages of manufacturing, as well as disposition and release of starting materials and customer facing Quality program leads for each client. The person filling this role
VeranovaContamination Control Specialist
This Contamination Control Specialist is the site SME responsible for coordinating all cleaning validation and verification activities related to intermediate and API manufacturing, including facility surfaces and equipment. This role involves close collaboration with various departments to ensure compliance with regulatory and customer requirements while implementing effective cleaning strategies across the site. The position is integral to maintaining quality and safety standards in the manufacturing
VeranovaMaintenance and Facilities Supervisor
The Maintenance and Facilities Supervisor oversees daily operations and performance of facilities and maintenance functions. This hands-on role includes managing routine maintenance and repairs for building systems, equipment, and infrastructure within the Pilot Plant—spanning HVAC, electrical, piping, and general facilities upkeep. The ideal candidate brings strong technical expertise and leadership to ensure safe, efficient, and reliable site operations. . Responsibilities cover the Devens, MA and North
VeranovaMaterial Planning Manager
This position will lead material planning, with direct responsibility for developing and managing processes and monitoring operating strategies in collaboration with cross-functional business partners. Utilizing SAVIOM, Excel, and Veranova’s ERP system, this role will integrate production planning, capacity planning, and manufacturing scheduling for a portfolio of client-owned products. Core Responsibilities: Design and implement a comprehensive monthly Sales and Operations Planning (S&OP) process from
VeranovaPharmaceutical Manufacturing Project Manager
The Senior Project Manager will lead cross-functional project teams to deliver complex CDMO (Contract Development and Manufacturing Organization) programs. This role is responsible for managing R&D and manufacturing activities, including seamless technology transfers between internal and client manufacturing sites. Serving as the primary point of contact for the client, the Senior Project Manager ensures alignment across all internal and external stakeholders. This position requires close collaboration
VeranovaProcess Engineer
The Process Engineer is responsible for the evaluation, design and implementation of elements of new or improved processes as they are transferred from development to production. The Process Engineer is also responsible for the monitoring of manufacturing processes while providing production support and ensuring compliance with safety and quality standards. Core Responsibilities:
VeranovaProduction Lead (Day Shift)
The Production Lead's principal responsibilities include operating production equipment, completing associated documentation, and directing production technicians on shift on the same duties. The Production Lead is responsible for ensuring that the shift meets all safety, compliance, and performance goals while meeting production schedules. The position also coordinates with other departments such as QA, QC, Purchasing, Maintenance, and Material Control to ensure all support activities are completed in a
VeranovaProduction Technician (Night Shift)
The Production Technician is responsible for the safe, cost effective, and timely manufacture of product that is fit for intended use and meets customer requirements and production schedule. Core Responsibilities: Completes batch records in accordance with FDA and Current Good Manufacturing Practices (cGMP) guidelines.Demonstrates technical proficiency and self-assuredness in applying cGMP standards.Provide process support and troubleshooting necessary to meet all customer requirements.Maintain the
VeranovaQuality Assurance (QA) Supervisor - Manufacturing
The QA Supervisor will coordinate with the Manager/Associate Director, Quality Assurance, the day-to-day activities of the Quality Assurance group in the support of the site’s Operations (manufacture, testing, shipment, etc.). This person will evaluate and implement systems, methods, techniques, and solutions to moderately complex quality and regulatory compliance issues, and be responsible for the leadership, development and training of team members within their oversight as well as providing supportive
VeranovaQuality Assurance Deviations Associate
The QA Deviations Associate will oversee the investigation, documentation, oversight, and resolution of deviations to ensure compliance with regulatory standards, internal policies, and industry best practices. The ideal candidate will bring expertise in deviation investigations for CGMP manufacturing and testing, an understanding of chemical processes for intermediates and APIs, a proactive problem-solving mindset, a coaching mindset, and a commitment to maintaining the highest standards of product
VeranovaQuality Assurance Document Control Specialist
We are seeking a Document Control Specialist to support the design, implementation, and maintenance of our Quality Assurance documentation system. This role manages the issuance, tracking, and control of GMP documents including SOPs, batch records, protocols, and reports, while administering quality documentation software. The ideal candidate will help ensure a compliant and well-maintained Quality Management System. Core Responsibilities:
VeranovaQuality Compliance Manager
This role is responsible for leading the Veranova Quality Systems & Compliance team. This role will oversee the compliance function and related processes for the multi-site New England region. The position manages and provides direction to Quality Systems and Compliance staff, ensuring that processes and activities are performed in compliance with company policies, procedures, standards and applicable local, state, federal, and international regulations relating to the manufacture of active
VeranovaScientist - Process Research & Development
The Scientist I - Process Research & Development (PRD) is responsible for conducting small to large scale chemical reactions to optimize synthetic routes of active pharmaceutical ingredients (APIs) under the direction of project technical leads to deliver projects on target with quantity, quality, time, and within budget. Core Responsibilities: Delivers experimental output with a high scientific integrity, both on time and target, and of high quality with guidance. Exhibits safety awareness, safely
VeranovaScientist - Process Research & Development
The Scientist I - Process Research & Development (PRD) is responsible for conducting small to large scale chemical reactions to optimize synthetic routes of active pharmaceutical ingredients (APIs) under the direction of project technical leads to deliver projects on target with quantity, quality, time, and within budget. Core Responsibilities: Delivers experimental output with a high scientific integrity, both on time and target, and of high quality with guidance. Exhibits safety awareness, safely
VeranovaSenior Quality Assurance Associate
The Senior QA Associate will perform on the floor walkthroughs of Manufacturing and Quality Control areas to drive Inspection Readiness activities. They will also perform review and release of Active Pharmaceutical Ingredients (APIs) in support of clinical and commercial product manufacturing, as well as assist in the development, implementation, and maintenance of quality systems and other Quality Assurance activities. This person must also maintain a high level of strict GMP compliance. Core
VeranovaSenior Scientist - Analytical R&D - Antibody Drug Conjugates
We are seeking a highly motivated and skilled Senior Scientist with experience in analyzing antibody drug conjugates (ADC) to join our ARD team in New England. The successful candidate will play a hands-on role in the development, qualification, transfer, and validation of analytical methods to support the development of ADC’s and other complex bioconjugates. Core Responsibilities: Collaborate with cross-functional teams to drive impactful projects. Exercise technical judgment in the planning,
VeranovaSupplier Quality Assurance Specialist
The Supplier Quality Assurance Specialist will evaluate, qualify and monitor the quality of external vendors providing Veranova materials, supplies and services impacting the quality of materials produced by Veranova. Core Responsibilities: Lead and perform supplier qualification activities including conducting audits, working with new and existing suppliers to help them understand Veranova’s quality requirements and close gaps in their quality systems or processesDrive supplier risk assessment
VeranovaTraining and Development Manager
The Training & Development Manager is responsible for designing, delivering, and managing a robust New England training program across the departments and the sites to help achieve the goal of providing outstanding education and training across the organization. Core Responsibilities: Develop, evaluate, and deliver high quality training programs across all functions and support external
VeranovaTraining Coordinator
The Training Specialist is responsible for designing, delivering, and managing training programs to help achieve the goal of providing outstanding education and training across the site. Core Responsibilities: Develop, evaluate, and deliver high-quality training programs across all functions and support external training by cross-functional teams.Design and develop employee training that
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